CA2146447C - Herbicide mixtures - Google Patents

Herbicide mixtures Download PDF

Info

Publication number: CA2146447C
Authority: CA; Canada
Prior art keywords: group; herbicide; component; pct; aryloxypicolinamide
Prior art date: 1992-10-06
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

CA002146447A

Other languages

English (en)

French (fr)

Other versions

CA2146447A1 (en

Inventor

Helmut Baltruschat

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Shell Internationale Research Maatschappij BV

Original Assignee

Shell Internationale Research Maatschappij BV

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1992-10-06

Filing date

1993-10-05

Publication date

2004-06-22

1993-10-05 Application filed by Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV

1994-04-14 Publication of CA2146447A1 publication Critical patent/CA2146447A1/en

2004-06-22 Application granted granted Critical

2004-06-22 Publication of CA2146447C publication Critical patent/CA2146447C/en

2013-10-05 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 49
239000004009 herbicide Substances 0.000 title claims abstract description 43
239000000203 mixture Substances 0.000 title claims description 18
241000196324 Embryophyta Species 0.000 claims abstract description 24
150000001875 compounds Chemical class 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 9
239000003666 Amidosulfuron Substances 0.000 claims description 7
CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 7
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims description 5
235000013339 cereals Nutrition 0.000 claims description 5
125000001188 haloalkyl group Chemical group 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims description 4
239000004480 active ingredient Substances 0.000 claims description 4
125000004414 alkyl thio group Chemical group 0.000 claims description 4
239000004202 carbamide Substances 0.000 claims description 4
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
239000005603 Prosulfocarb Substances 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical group CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims description 3
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims description 3
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 3
OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 claims description 2
CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 claims description 2
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 2
HTPXFGUCAUTOEL-UHFFFAOYSA-N 9h-fluorene-1-carboxylic acid Chemical compound C1C2=CC=CC=C2C2=C1C(C(=O)O)=CC=C2 HTPXFGUCAUTOEL-UHFFFAOYSA-N 0.000 claims description 2
239000002890 Aclonifen Substances 0.000 claims description 2
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 2
239000005489 Bromoxynil Substances 0.000 claims description 2
239000005506 Diclofop Substances 0.000 claims description 2
GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 claims description 2
239000005558 Fluroxypyr Substances 0.000 claims description 2
239000005573 Linuron Substances 0.000 claims description 2
239000005574 MCPA Substances 0.000 claims description 2
CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 claims description 2
239000005591 Pendimethalin Substances 0.000 claims description 2
239000005606 Pyridate Substances 0.000 claims description 2
JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 2
DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000003302 alkenyloxy group Chemical group 0.000 claims description 2
125000005108 alkenylthio group Chemical group 0.000 claims description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
125000005109 alkynylthio group Chemical group 0.000 claims description 2
125000003368 amide group Chemical group 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 2
125000004438 haloalkoxy group Chemical group 0.000 claims description 2
125000004995 haloalkylthio group Chemical group 0.000 claims description 2
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 2
LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims description 2
IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 claims description 2
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
125000005133 alkynyloxy group Chemical group 0.000 claims 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
125000005415 substituted alkoxy group Chemical group 0.000 claims 1
241000894007 species Species 0.000 abstract description 6
238000001228 spectrum Methods 0.000 abstract description 3
238000011282 treatment Methods 0.000 description 10
238000009303 advanced oxidation process reaction Methods 0.000 description 9
230000000694 effects Effects 0.000 description 6
230000002195 synergetic effect Effects 0.000 description 5
239000002689 soil Substances 0.000 description 4
240000005979 Hordeum vulgare Species 0.000 description 3
235000007340 Hordeum vulgare Nutrition 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
230000009036 growth inhibition Effects 0.000 description 3
238000012360 testing method Methods 0.000 description 3
241001621841 Alopecurus myosuroides Species 0.000 description 2
241001666377 Apera Species 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
230000009418 agronomic effect Effects 0.000 description 2
-1 cyano, carboxy Chemical group 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
229910052731 fluorine Chemical group 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 1
241000602336 Anthemis arvensis Species 0.000 description 1
244000116566 Aphanes arvensis Species 0.000 description 1
235000002083 Aphanes arvensis Nutrition 0.000 description 1
241000534456 Arenaria <Aves> Species 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
241000544808 Bromus sterilis Species 0.000 description 1
101150110592 CTS1 gene Proteins 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
241000271942 Cerastes Species 0.000 description 1
241000219312 Chenopodium Species 0.000 description 1
240000001579 Cirsium arvense Species 0.000 description 1
235000005918 Cirsium arvense Nutrition 0.000 description 1
241001289540 Fallopia convolvulus Species 0.000 description 1
241001508646 Galeopsis tetrahit Species 0.000 description 1
240000005702 Galium aparine Species 0.000 description 1
235000014820 Galium aparine Nutrition 0.000 description 1
241000004701 Geranium dissectum Species 0.000 description 1
206010061217 Infestation Diseases 0.000 description 1
244000303225 Lamium amplexicaule Species 0.000 description 1
235000009198 Lamium amplexicaule Nutrition 0.000 description 1
240000006503 Lamium purpureum Species 0.000 description 1
235000009193 Lamium purpureum Nutrition 0.000 description 1
241001492668 Legousia hybrida Species 0.000 description 1
240000004296 Lolium perenne Species 0.000 description 1
244000234597 Montia perfoliata Species 0.000 description 1
235000001851 Montia perfoliata Nutrition 0.000 description 1
241001442135 Myosotis arvensis Species 0.000 description 1
101100045754 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) rtf-1 gene Proteins 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
240000004674 Papaver rhoeas Species 0.000 description 1
235000007846 Papaver rhoeas Nutrition 0.000 description 1
240000006928 Persicaria lapathifolia Species 0.000 description 1
241000257649 Phalaris minor Species 0.000 description 1
241000461749 Phalaris paradoxa Species 0.000 description 1
244000292693 Poa annua Species 0.000 description 1
240000006597 Poa trivialis Species 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
240000003705 Senecio vulgaris Species 0.000 description 1
240000000022 Silene vulgaris Species 0.000 description 1
235000011312 Silene vulgaris Nutrition 0.000 description 1
240000003728 Spergula arvensis Species 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
241000404538 Tripleurospermum maritimum subsp. inodorum Species 0.000 description 1
240000000359 Triticum dicoccon Species 0.000 description 1
241000990144 Veronica persica Species 0.000 description 1
241000394440 Viola arvensis Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
239000011149 active material Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
238000011278 co-treatment Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000007429 general method Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
AHLBNYSZXLDEJQ-FWEHEUNISA-N orlistat Chemical compound CCCCCCCCCCC[C@H](OC(=O)[C@H](CC(C)C)NC=O)C[C@@H]1OC(=O)[C@H]1CCCCCC AHLBNYSZXLDEJQ-FWEHEUNISA-N 0.000 description 1
230000002688 persistence Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CA002146447A 1992-10-06 1993-10-05 Herbicide mixtures Expired - Lifetime CA2146447C (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
EP92117054		1992-10-06
EP92117054.4		1992-10-06
PCT/EP1993/002737 WO1994007368A1 (en)	1992-10-06	1993-10-05	Herbicide mixtures

Publications (2)

Publication Number	Publication Date
CA2146447A1 CA2146447A1 (en)	1994-04-14
CA2146447C true CA2146447C (en)	2004-06-22

Family

ID=8210104

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002146447A Expired - Lifetime CA2146447C (en)	1992-10-06	1993-10-05	Herbicide mixtures

Country Status (23)

Country	Link
US (1)	US5674807A (pl)
EP (1)	EP0665715B1 (pl)
JP (1)	JP3794695B2 (pl)
KR (1)	KR100297335B1 (pl)
CN (1)	CN1074646C (pl)
AT (1)	ATE147228T1 (pl)
AU (1)	AU671866B2 (pl)
BR (1)	BR9307184A (pl)
CA (1)	CA2146447C (pl)
CZ (1)	CZ284355B6 (pl)
DE (2)	DE122005000059I2 (pl)
DK (1)	DK0665715T3 (pl)
ES (1)	ES2096950T3 (pl)
GR (1)	GR3022354T3 (pl)
HK (1)	HK1000342A1 (pl)
HU (1)	HU218170B (pl)
MD (1)	MD1753B2 (pl)
PL (7)	PL173183B1 (pl)
RO (1)	RO115011B1 (pl)
RU (1)	RU2125370C1 (pl)
SK (1)	SK281066B6 (pl)
UA (1)	UA43325C2 (pl)
WO (1)	WO1994007368A1 (pl)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5977026A (en) *	1996-07-30	1999-11-02	American Cyanamid	Herbicidal mixtures
US5985796A (en) *	1998-01-22	1999-11-16	American Cyanamid Company	Herbicidal mixtures
GB9914213D0 (en) *	1999-06-17	1999-08-18	Rhone Poulenc Agrochimie	New herbicidal compositions
US6348434B1 (en) *	1999-07-01	2002-02-19	Basf Aktiengesellschaft	Herbicidal emulsifiable concentrate
CZ20021306A3 (cs) *	1999-10-14	2003-01-15	Basf Corporation	Synergické herbicidní způsoby a kompozice
EP1351571A2 (de) *	1999-11-17	2003-10-15	Bayer CropScience AG	Selektive herbizide auf basis von 2,6-disubstituierten pyridin-derivaten
CN100488362C (zh) *	2000-01-25	2009-05-20	辛根塔参与股份公司	除草组合物
HUP0300564A3 (en) *	2000-04-04	2005-11-28	Basf Ag	Synergistic herbicidal composition and its use
DE10135641A1 (de) *	2001-07-21	2003-02-06	Bayer Cropscience Gmbh	Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen
DE10135642A1 (de) *	2001-07-21	2003-02-27	Bayer Cropscience Gmbh	Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen
GT200300290A (es) *	2002-12-30	2004-10-13		Herbicidas novedosos
DE10307078A1 (de) *	2003-02-19	2004-09-09	Bayer Cropscience Gmbh	Verfahren zur Herstellung von wasserdispergierbaren Granulaten
BRPI0408232A (pt)	2003-03-13	2006-03-01	Basf Ag	mistura e composição herbicidas, processo para a preparação de composições herbicidas, e, método para o controle de vegetação indesejável
ATE336900T1 (de) *	2003-03-13	2006-09-15	Basf Ag	Synergistisch wirkende herbizide mischungen
MXPA05009189A (es)	2003-03-13	2005-10-18	Basf Ag	Mezclas herbicidas.
EP1827106A2 (en) *	2004-12-17	2007-09-05	Syngeta Participations AG	Herbicidal compositions comprising prosulfocars
AR071339A1 (es) *	2008-02-05	2010-06-16	Arysta Lifescience North Ameri	Formulacion solida de compuesto activo de baja fusion
WO2014138561A1 (en)	2013-03-08	2014-09-12	Dow Agrosciences Llc	Herbicidal compositions comprising isoxaben and aminopyralid
JP7063231B2 (ja) *	2018-10-26	2022-05-09	住友化学株式会社	ジピリダジニルエーテル化合物及びその用途

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GR861640B (en) *	1985-07-02	1986-10-24	May & Baker Ltd	Insecticide method by using diflufenican
GR861894B (en) *	1985-07-23	1986-11-24	May & Baker Ltd	Herbicidal method comprising the use of diflufenican
US5264411A (en) *	1985-07-23	1993-11-23	May & Baker Limited	Herbicidal method comprising the use of diflufenican
GB8526735D0 (en) *	1985-10-30	1985-12-04	May & Baker Ltd	Compositions of matter
GB8617740D0 (en) *	1986-07-21	1986-08-28	May & Baker Ltd	Compositions of matter
GB8617741D0 (en) *	1986-07-21	1986-08-28	May & Baker Ltd	Compositions of matter
GB8630698D0 (en) *	1986-12-23	1987-02-04	May & Baker Ltd	Compositions of matter
GB8630806D0 (en) *	1986-12-23	1987-02-04	May & Baker Ltd	Compositions of matter
FR2611437A1 (fr) *	1987-03-05	1988-09-09	Rhone Poulenc Agrochimie	Produit herbicide resultant de l'association de l'aclonifen avec l'oxadiazon ou le diflufenican
GB9005965D0 (en) *	1990-03-16	1990-05-09	Shell Int Research	Herbicidal carboxamide derivatives
GB9025828D0 (en) *	1990-11-28	1991-01-09	Shell Int Research	Herbicidal carboxamide derivatives
TW212792B (pl) *	1991-09-13	1993-09-11	Shell Internat Res Schappej B V

1993
- 1993-10-04 CN CN93118252A patent/CN1074646C/zh not_active Expired - Lifetime
- 1993-10-05 AT AT93922914T patent/ATE147228T1/de active
- 1993-10-05 KR KR1019950700546A patent/KR100297335B1/ko not_active Expired - Fee Related
- 1993-10-05 BR BR9307184A patent/BR9307184A/pt not_active IP Right Cessation
- 1993-10-05 HK HK97101934A patent/HK1000342A1/en not_active IP Right Cessation
- 1993-10-05 PL PL93319748A patent/PL173183B1/pl unknown
- 1993-10-05 RU RU95110769A patent/RU2125370C1/ru active
- 1993-10-05 MD MD96-0315A patent/MD1753B2/ro unknown
- 1993-10-05 AU AU51759/93A patent/AU671866B2/en not_active Expired
- 1993-10-05 UA UA95048306A patent/UA43325C2/uk unknown
- 1993-10-05 DE DE122005000059C patent/DE122005000059I2/de active Active
- 1993-10-05 US US08/406,989 patent/US5674807A/en not_active Expired - Lifetime
- 1993-10-05 JP JP50873294A patent/JP3794695B2/ja not_active Expired - Lifetime
- 1993-10-05 PL PL93319749A patent/PL173188B1/pl unknown
- 1993-10-05 ES ES93922914T patent/ES2096950T3/es not_active Expired - Lifetime
- 1993-10-05 CA CA002146447A patent/CA2146447C/en not_active Expired - Lifetime
- 1993-10-05 EP EP93922914A patent/EP0665715B1/en not_active Expired - Lifetime
- 1993-10-05 DK DK93922914.2T patent/DK0665715T3/da active
- 1993-10-05 PL PL93319744A patent/PL173179B1/pl unknown
- 1993-10-05 DE DE69307335T patent/DE69307335T2/de not_active Expired - Lifetime
- 1993-10-05 PL PL93308246A patent/PL173338B1/pl unknown
- 1993-10-05 RO RO95-00650A patent/RO115011B1/ro unknown
- 1993-10-05 SK SK406-95A patent/SK281066B6/sk not_active IP Right Cessation
- 1993-10-05 PL PL93319746A patent/PL173185B1/pl unknown
- 1993-10-05 PL PL93319747A patent/PL173184B1/pl unknown
- 1993-10-05 WO PCT/EP1993/002737 patent/WO1994007368A1/en not_active Ceased
- 1993-10-05 HU HU9500992A patent/HU218170B/hu active IP Right Revival
- 1993-10-05 CZ CZ95610A patent/CZ284355B6/cs not_active IP Right Cessation
- 1993-10-05 PL PL93319745A patent/PL173190B1/pl unknown
1997
- 1997-01-23 GR GR960401770T patent/GR3022354T3/el unknown

Also Published As

Publication number	Publication date
CA2146447A1 (en)	1994-04-14
PL308246A1 (en)	1995-07-24
PL173179B1 (pl)	1998-02-27
PL173338B1 (pl)	1998-02-27
ES2096950T3 (es)	1997-03-16
GR3022354T3 (en)	1997-04-30
UA43325C2 (uk)	2001-12-17
BR9307184A (pt)	1999-03-30
DE69307335T2 (de)	1997-04-30
WO1994007368A1 (en)	1994-04-14
HU9500992D0 (en)	1995-06-28
CZ284355B6 (cs)	1998-11-11
RU2125370C1 (ru)	1999-01-27
SK281066B6 (sk)	2000-11-07
PL173185B1 (pl)	1998-02-27
JP3794695B2 (ja)	2006-07-05
HU218170B (hu)	2000-06-28
SK40695A3 (en)	1995-07-11
JPH08501782A (ja)	1996-02-27
PL173183B1 (pl)	1998-02-27
EP0665715A1 (en)	1995-08-09
US5674807A (en)	1997-10-07
AU671866B2 (en)	1996-09-12
ATE147228T1 (de)	1997-01-15
DE69307335D1 (de)	1997-02-20
KR100297335B1 (ko)	2001-11-30
CZ61095A3 (en)	1995-10-18
DE122005000059I2 (de)	2011-01-20
DK0665715T3 (da)	1997-01-27
RU95110769A (ru)	1996-12-27
PL173188B1 (pl)	1998-02-27
PL173190B1 (pl)	1998-02-27
AU5175993A (en)	1994-04-26
PL173184B1 (pl)	1998-02-27
CN1086080A (zh)	1994-05-04
HUT70088A (en)	1995-09-28
MD1753B2 (ro)	2001-10-31
CN1074646C (zh)	2001-11-14
RO115011B1 (ro)	1999-10-29
HK1000342A1 (en)	1998-03-06
EP0665715B1 (en)	1997-01-08

Legal Events

Date	Code	Title	Description
2000-09-21	EEER	Examination request
2013-12-09	MKEX	Expiry	Effective date: 20131007

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